与Plectin (PLEC)相关的中度大疱性表皮松解症,无皮外受损伤,对氨苯砜有应答。

IF 2 Q3 DERMATOLOGY
Indian Dermatology Online Journal Pub Date : 2025-09-01 Epub Date: 2025-08-19 DOI:10.4103/idoj.idoj_1064_24
Anisha Biswal, Bikash Ranjan Kar, Rahul Mahajan, Liza Mohapatra, Anoop Kumar
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引用次数: 0

摘要

摘要:凝集素病是由凝集素基因(PLEC)突变引起的一系列疾病,具有广泛的表现,主要表现为皮肤外,如幽门闭锁、肌肉萎缩、心肌病,并伴有皮肤紧张性水疱。不同剪接的外显子产生不同的异构体,这些异构体在不同的细胞类型和组织中具有明确的功能。我们报告一个14岁的女孩,从童年开始就表现出四肢和躯干的紧张性瘙痒性囊泡和大疱的特征。她被诊断为中度单纯大疱性表皮松解症,在1号外显子有无意义的PLEC突变。该病例的独特之处在于没有皮肤外表现和她对氨苯砜的戏剧性反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Plectin ( PLEC )-Related Intermediate Epidermolysis Bullosa Simplex without Extracutaneous Involvement with Response to Dapsone.

Plectin ( PLEC )-Related Intermediate Epidermolysis Bullosa Simplex without Extracutaneous Involvement with Response to Dapsone.

Plectin ( PLEC )-Related Intermediate Epidermolysis Bullosa Simplex without Extracutaneous Involvement with Response to Dapsone.

Abstract: Plectinopathies, the spectrum of diseases caused by plectin gene ( PLEC ) mutations, have a wide range of manifestations, mostly extracutaneous, like pyloric atresia, muscular dystrophy, and cardiomyopathy, along with cutaneous tense blistering. Differently spliced exons give rise to various isoforms, which have definitive functions in different cell types and tissues. We report a case of a 14-year-old girl presenting with features of tense pruritic vesicles and bullae on extremities and trunk since childhood. She was diagnosed with intermediate epidermolysis bullosa simplex, having nonsense PLEC mutation at exon 1. The uniqueness of the case is the absence of extracutaneous manifestations and her dramatic response to dapsone.

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来源期刊
CiteScore
2.00
自引率
11.80%
发文量
201
审稿时长
49 weeks
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